NDC 68083-515
Octreotide Acetate 200 ug per 1 mL injection, solution
On the label: Gland Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyJun 27, 2023 · 4 inspections |
Product details
- Generic drug
- Octreotide: every company that makes it
- Form
- injection, solution, intravenous; subcutaneous
- Strength
- 200 ug per 1 mL
- Approval
- ANDA ANDA216807
- On the market since
- Jun 13, 2023
- Package NDCs
68083-515-01- Official label
- DailyMed (National Library of Medicine), updated Jul 25, 2024
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